Variant report

Variant rs73346898
Chromosome Location chr8:126532733-126532734
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:126518000-126534400 Weak transcription Right Atrium heart
2 chr8:126525800-126538800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr8:126526000-126534200 Weak transcription Ovary ovary
4 chr8:126526000-126537400 Weak transcription Fetal Lung lung
5 chr8:126526200-126534400 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr8:126527000-126538200 Weak transcription Placenta Amnion Placenta Amnion
7 chr8:126527400-126534400 Weak transcription Osteobl bone
8 chr8:126527600-126537000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr8:126528000-126537200 Weak transcription Psoas Muscle Psoas
10 chr8:126528600-126537000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr8:126528600-126537000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr8:126529000-126533400 Weak transcription Primary monocytes fromperipheralblood blood
13 chr8:126529400-126534600 Weak transcription Adipose Nuclei Adipose
14 chr8:126529400-126537000 Weak transcription Liver Liver
15 chr8:126530600-126533400 Weak transcription Esophagus oesophagus
16 chr8:126532000-126536200 Weak transcription Hela-S3 cervix
17 chr8:126532000-126537000 Weak transcription A549 lung
18 chr8:126532000-126537000 Weak transcription NHEK skin
19 chr8:126532200-126533400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
20 chr8:126532200-126537000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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